Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Multicenter Study
. 2018 Jul;142(1):e20174058.
doi: 10.1542/peds.2017-4058.

Preterm Neuroimaging and School-Age Cognitive Outcomes

Affiliations
Multicenter Study

Preterm Neuroimaging and School-Age Cognitive Outcomes

Susan R Hintz et al. Pediatrics. 2018 Jul.

Abstract

Background and objectives: Children born extremely preterm are at risk for cognitive difficulties and disability. The relative prognostic value of neonatal brain MRI and cranial ultrasound (CUS) for school-age outcomes remains unclear. Our objectives were to relate near-term conventional brain MRI and early and late CUS to cognitive impairment and disability at 6 to 7 years among children born extremely preterm and assess prognostic value.

Methods: A prospective study of adverse early and late CUS and near-term conventional MRI findings to predict outcomes at 6 to 7 years including a full-scale IQ (FSIQ) <70 and disability (FSIQ <70, moderate-to-severe cerebral palsy, or severe vision or hearing impairment) in a subgroup of Surfactant Positive Airway Pressure and Pulse Oximetry Randomized Trial enrollees. Stepwise logistic regression evaluated associations of neuroimaging with outcomes, adjusting for perinatal-neonatal factors.

Results: A total of 386 children had follow-up. In unadjusted analyses, severity of white matter abnormality and cerebellar lesions on MRI and adverse CUS findings were associated with outcomes. In full regression models, both adverse late CUS findings (odds ratio [OR] 27.9; 95% confidence interval [CI] 6.0-129) and significant cerebellar lesions on MRI (OR 2.71; 95% CI 1.1-6.7) remained associated with disability, but only adverse late CUS findings (OR 20.1; 95% CI 3.6-111) were associated with FSIQ <70. Predictive accuracy of stepwise models was not substantially improved with the addition of neuroimaging.

Conclusions: Severe but rare adverse late CUS findings were most strongly associated with cognitive impairment and disability at school age, and significant cerebellar lesions on MRI were associated with disability. Near-term conventional MRI did not substantively enhance prediction of severe early school-age outcomes.

PubMed Disclaimer

Conflict of interest statement

POTENTIAL CONFLICT OF INTEREST: The authors have indicated they have no potential conflicts of interest to disclose.

Figures

FIGURE 1
FIGURE 1
Independent associations of neonatal neuroimaging findings with cognitive impairment and moderate-to-severe disability at early school age. A, FSIQ <70. B, Moderate-to-severe disability. Early CUS composite adverse finding was defined as grade III or IV ICH or cPVL. Late CUS composite adverse finding was defined as moderate or severe VE, cPVL, porencephalic cyst, or shunt. The full model included the following perinatal, neonatal, and sociodemographic factors that were associated with P < .2 in backward stepwise models: FSIQ <70: male sex (OR: 2.07; 95% CI 1.0–4.28; P = .049), maternal education less than high school (OR: 2.05; 95% CI 0.98–4.29; P = .056), BPD (OR: 1.59; 95% CI 0.78–3.23; P = .20); moderate-severe disability: male sex (OR: 1.93; 95% CI 0.98–3.80; P = .057), BPD (OR: 1.30; 95% CI 0.67–2.50; P = .44). Limited model 1 includes perinatal and neonatal factors, early CUS, and brain MRI (excludes late CUS); limited model 2 includes perinatal and neonatal factors, early CUS, and late CUS (excludes MRI). * P < .05; *** P < .001.

Comment in

References

    1. Hutchinson EA, De Luca CR, Doyle LW, Roberts G, Anderson PJ; Victorian Infant Collaborative Study Group . School-age outcomes of extremely preterm or extremely low birth weight children. Pediatrics. 2013;131(4). Available at: www.pediatrics.org/cgi/content/full/131/4/e1053 - PubMed
    1. Spittle AJ, Cheong J, Doyle LW, et al. . Neonatal white matter abnormality predicts childhood motor impairment in very preterm children. Dev Med Child Neurol. 2011;53(11):1000–1006 - PMC - PubMed
    1. Serenius F, Ewald U, Farooqi A, et al. ; Extremely Preterm Infants in Sweden Study Group . Neurodevelopmental outcomes among extremely preterm infants 6.5 years after active perinatal care in Sweden. JAMA Pediatr. 2016;170(10):954–963 - PubMed
    1. Johnson S, Strauss V, Gilmore C, Jaekel J, Marlow N, Wolke D. Learning disabilities among extremely preterm children without neurosensory impairment: comorbidity, neuropsychological profiles and scholastic outcomes. Early Hum Dev. 2016;103:69–75 - PubMed
    1. Stoll BJ, Hansen NI, Bell EF, et al. ; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network . Trends in care practices, morbidity, and mortality of extremely preterm neonates, 1993-2012. JAMA. 2015;314(10):1039–1051 - PMC - PubMed

Publication types

LinkOut - more resources